A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1024225



Internal ID16318181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9999034..10055804hg38UCSC Ensembl
Innerchr5:9999146..10055916hg19UCSC Ensembl
Innerchr5:10052146..10108916hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3856771
hg1956771
hg1856771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597109
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1024225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer